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Lista de obras de Carole Ober

(Too) great expectations: the challenges in replicating asthma disease genes

artículo científico publicado en 2009

116 Genome-Wide Association Studies of Asthma Indicate Opposite Immunopathogenesis Direction From Autoimmune Diseases.

artículo científico publicado en 2012

A LASSO penalized regression approach for genome-wide association analyses using related individuals: application to the Genetic Analysis Workshop 19 simulated data

artículo científico publicado en 2016

A common cortactin gene variation confers differential susceptibility to severe asthma

artículo científico publicado en 2008

A common spinal muscular atrophy deletion mutation is present on a single founder haplotype in the US Hutterites

artículo científico publicado en 2011

A common variant associated with prostate cancer in European and African populations

artículo científico publicado en 2006

A common variant in RAB27A gene is associated with fractional exhaled nitric oxide levels in adults

artículo científico publicado en 2015

A comparison of humans and baboons suggests germline mutation rates do not track cell divisions

scientific article published on 17 August 2020

A continuum of admixture in the Western Hemisphere revealed by the African Diaspora genome

scientific article published on 11 October 2016

A decade of research on the 17q12-21 asthma locus: Piecing together the puzzle.

artículo científico publicado en 2018

A genome-wide screen for hyposmia susceptibility Loci

artículo científico publicado en 2008

A genome-wide search for quantitative trait loci contributing to variation in seasonal pollen reactivity

scientific article published on 01 January 2006

A genome-wide survey of CD4(+) lymphocyte regulatory genetic variants identifies novel asthma genes

artículo científico publicado en 2014

A genomewide screen for chronic rhinosinusitis genes identifies a locus on chromosome 7q.

artículo científico publicado en 2008

A meta-analysis of genome-wide association studies for serum total IgE in diverse study populations

artículo científico publicado en 2012

A multiple splitting approach to linkage analysis in large pedigrees identifies a linkage to asthma on chromosome 12.

artículo científico publicado en 2009

A novel NDUFS4 frameshift mutation causes Leigh disease in the Hutterite population

artículo científico publicado en 2016

A population-based study of autosomal-recessive disease-causing mutations in a founder population

artículo científico publicado en 2012

A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch-German) Mennonite and Hutterite patients in North America.

artículo científico publicado en 2012

A variant of the myosin light chain kinase gene is associated with severe asthma in African Americans

artículo científico publicado en 2007

Accurate imputation of rare and common variants in a founder population from a small number of sequenced individuals

artículo científico publicado en 2012

Allele-Specific Targeting of microRNAs to HLA-G and Risk of Asthma

article

Allele-specific targeting of microRNAs to HLA-G and risk of asthma

artículo científico publicado en 2007

Amish and Hutterite Environmental Farm Products Have Opposite Effects on Experimental Models of Asthma

artículo científico publicado en 2016

An admixture mapping meta-analysis implicates genetic variation at 18q21 with asthma susceptibility in Latinos

scientific article published on 07 September 2018

An estimate of the average number of recessive lethal mutations carried by humans

artículo científico publicado en 2015

An siRNA-based functional genomics screen for the identification of regulators of ciliogenesis and ciliopathy genes ⬇️

scientific journal article

Are common disease susceptibility alleles the same in outbred and founder populations?

scientific article published on 01 July 2004

Assembly of a pan-genome from deep sequencing of 910 humans of African descent

Association of ORMDL3 with rhinovirus-induced endoplasmic reticulum stress and type I Interferon responses in human leucocytes.

artículo científico publicado en 2017

Association studies for asthma and atopic diseases: a comprehensive review of the literature

artículo científico publicado en 2003

Association study in African-admixed populations across the Americas recapitulates asthma risk loci in non-African populations

artículo científico publicado en 2019

Associations of autozygosity with a broad range of human phenotypes

scientific article published on 31 October 2019

Asthma Genetics in the Post-GWAS Era.

artículo científico publicado en 2016

Asthma genetics 2006: the long and winding road to gene discovery.

artículo científico publicado en 2006

Author Correction: Assembly of a pan-genome from deep sequencing of 910 humans of African descent

scientific article published on 01 February 2019

Author Correction: Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

artículo científico publicado en 2018

Best linear unbiased allele-frequency estimation in complex pedigrees

artículo científico publicado en 2004

Blood groups in the species survival plan®, European endangered species program, and managed in situ populations of bonobo (Pan paniscus), common chimpanzee (Pan troglodytes), gorilla (Gorilla ssp.), and orangutan (Pongo pygmaeus ssp.) ⬇️

artículo científico publicado el 17 de septiembre de 2010

Broad-scale recombination patterns underlying proper disjunction in humans

artículo científico publicado en 2009

CDHR3 Genetics and Rhinovirus C Respiratory Illnesses

artículo científico publicado en 2017

CFTR mutations and reproductive outcomes in a population isolate

Characterization of a Unique Form of Arrhythmic Cardiomyopathy Caused by Recessive Mutation in LEMD2

Colloquium papers: Heritability of reproductive fitness traits in a human population

artículo científico publicado en 2009

Common sequence variants on 2p15 and Xp11.22 confer susceptibility to prostate cancer

scientific journal article

Correlation of intergenerational family sizes suggests a genetic component of reproductive fitness

artículo científico publicado en 2007

Cutting edge: polymorphisms in the ICOS promoter region are associated with allergic sensitization and Th2 cytokine production

artículo científico publicado en 2005

DNA methylation in lung cells is associated with asthma endotypes and genetic risk

artículo científico publicado en 2016

Determining the genetic basis of anthracycline-cardiotoxicity by molecular response QTL mapping in induced cardiomyocytes

Determining the genetic basis of anthracycline-cardiotoxicity by molecular response QTL mapping in induced cardiomyocytes.

artículo científico publicado en 2018

Development of a diagnostic DNA chip to screen for 30 autosomal recessive disorders in the Hutterite population

artículo científico publicado en 2016

Directional dominance on stature and cognition in diverse human populations

artículo científico publicado en 2015

Disclosure of genetic research results to members of a founder population

artículo científico publicado en 2014

Does HLA-dependent chimerism underlie the pathogenesis of juvenile dermatomyositis?

artículo científico publicado en 2004

Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes

artículo científico publicado en 2010

Drawing the history of the Hutterite population on a genetic landscape: inference from Y-chromosome and mtDNA genotypes.

artículo científico publicado en 2010

Effect of variation in CHI3L1 on serum YKL-40 level, risk of asthma, and lung function

artículo científico publicado en 2008

Effects of an FcγRIIA polymorphism on leukocyte gene expression and cytokine responses to anti-CD3 and anti-CD28 antibodies

artículo científico publicado en 2018

Effects of dog ownership and genotype on immune development and atopy in infancy

artículo científico publicado en 2004

Elevated levels of soluble humanleukocyte antigen-G in the airways are a marker for a low-inflammatory endotype of asthma.

artículo científico publicado en 2017

Empirical data about women's attitudes toward a biobank focused on pregnancy outcomes

artículo científico publicado en 2008

Empirical data about women's attitudes towards a hypothetical pediatric biobank

artículo científico publicado en 2008

Epigenome-Wide Association Study of DNA Methylation and Adult Asthma in the Agricultural Lung Health Study

artículo científico publicado en 2020

Epigenome-wide analysis links SMAD3 methylation at birth to asthma in children of asthmatic mothers

artículo científico publicado en 2016

Estimating the human mutation rate using autozygosity in a founder population

artículo científico publicado en 2012

Ethnic-specific associations of rare and low-frequency DNA sequence variants with asthma

artículo científico publicado en 2015

Evaluating the evidence for transmission distortion in human pedigrees

artículo científico publicado en 2012

Evidence for an IL-6-high asthma phenotype in asthmatic patients of African ancestry

scientific article published on 25 April 2019

Evidence for extensive transmission distortion in the human genome

artículo científico publicado en 2003

Evidence for gene-environment interactions in a linkage study of asthma and smoking exposure

artículo científico publicado en 2003

Evidence of balancing selection at the HLA-G promoter region.

artículo científico publicado en 2005

Evolutionary forward genomics reveals novel insights into the genes and pathways dysregulated in recurrent early pregnancy loss

artículo científico publicado en 2015

Evolutionary genetics of the human Rh blood group system

artículo científico publicado en 2012

Exome sequencing and the genetics of intellectual disability.

artículo científico publicado en 2011

Exome sequencing reveals a novel mutation for autosomal recessive non-syndromic mental retardation in the TECR gene on chromosome 19p13

artículo científico publicado en 2011

Expression Quantitative Trait Locus Mapping Studies in Mid-secretory Phase Endometrial Cells Identifies HLA-F and TAP2 as Fecundability-Associated Genes

artículo científico publicado en 2016

Fine mapping and positional candidate studies identify HLA-G as an asthma susceptibility gene on chromosome 6p21

artículo científico publicado en 2004

Fine mapping and positional candidate studies on chromosome 5p13 identify multiple asthma susceptibility loci

artículo científico publicado en 2006

Fine mapping of a locus for nonsyndromic mental retardation on chromosome 19p13

artículo científico publicado en 2008

Fraction of exhaled nitric oxide values in childhood are associated with 17q11.2-q12 and 17q12-q21 variants

artículo científico publicado en 2013

From the Cover: Whole-genome association study identifies STK39 as a hypertension susceptibility gene.

artículo científico publicado en 2008

Functional variants of the sphingosine-1-phosphate receptor 1 gene associate with asthma susceptibility

artículo científico publicado en 2010

Further replication studies of the EVE Consortium meta-analysis identifies 2 asthma risk loci in European Americans

artículo científico publicado en 2012

Future Research Directions in Asthma. An NHLBI Working Group Report

artículo científico publicado en 2015

Gene Coexpression Networks in Whole Blood Implicate Multiple Interrelated Molecular Pathways in Obesity in People with Asthma

scholarly article by Damien C Croteau-Chonka et al published 25 October 2018 in Obesity

Gene Expression Profiling in Blood Provides Reproducible Molecular Insights into Asthma Control

artículo científico publicado en 2016

Gene co-expression networks in whole blood implicate multiple interrelated molecular pathways in obese asthma

article

Gene-environment interaction effects on the development of immune responses in the 1st year of life

artículo científico publicado en 2005

Gene-environment interactions in human disease: nuisance or opportunity?

artículo científico publicado en 2011

Genetic Determinants of the Gut Microbiome in UK Twins

artículo científico publicado en 2016

Genetic associations with viral respiratory illnesses and asthma control in children.

artículo científico publicado en 2015

Genetic studies of stuttering in a founder population

artículo científico publicado en 2006

Genetic variance components estimation for binary traits using multiple related individuals

artículo científico publicado en 2011

Genetic variation in immunoregulatory pathways and atopic phenotypes in infancy

artículo científico publicado en 2004

Genetic-Epigenetic Interactions in Asthma Revealed by a Genome-Wide Gene-Centric Search

artículo científico publicado en 2018

Genome scan for loci linked to mite sensitivity: the Collaborative Study on the Genetics of Asthma (CSGA)

scientific article published on 01 May 2004

Genome-Wide Association Studies of the Human Gut Microbiota

artículo científico publicado en 2015

Genome-Wide Association Study Identification of Novel Loci Associated with Airway Responsiveness in Chronic Obstructive Pulmonary Disease

artículo científico publicado en 2015

Genome-Wide Methylation Study Identifies an IL-13-induced Epigenetic Signature in Asthmatic Airways

artículo científico publicado en 2015

Genome-wide ancestry association testing identifies a common European variant on 6q14.1 as a risk factor for asthma in African American subjects

artículo científico publicado en 2012

Genome-wide association and HLA fine-mapping studies identify risk loci and genetic pathways underlying allergic rhinitis

scholarly article by Johannes Waage et al published August 2018 in Nature Genetics

Genome-wide association studies of asthma indicate opposite immunopathogenesis direction from autoimmune diseases

artículo científico publicado en 2012

Genome-wide association study and admixture mapping reveal new loci associated with total IgE levels in Latinos

artículo científico publicado en 2014

Genome-wide association study identifies ITGB3 as a QTL for whole blood serotonin

artículo científico publicado en 2004

Genome-wide association study identifies a second prostate cancer susceptibility variant at 8q24.

artículo científico publicado en 2007

Genome-wide association study identifies candidate genes for male fertility traits in humans

artículo científico publicado en 2012

Genome-wide association study of lung function phenotypes in a founder population

artículo científico publicado en 2013

Genome-wide association study of plasma lipoprotein(a) levels identifies multiple genes on chromosome 6q

artículo científico publicado en 2009

Genome-wide association study of recalcitrant atopic dermatitis in Korean children

artículo científico publicado en 2015

Genome-wide interaction studies reveal sex-specific asthma risk alleles

artículo científico publicado en 2014

Getting from genes to function in lung disease: a National Heart, Lung, and Blood Institute workshop report

artículo científico publicado en 2010

Global DNA methylation changes spanning puberty are near predicted estrogen-responsive genes and enriched for genes involved in endocrine and immune processes.

artículo científico publicado en 2018

HLA-G and immune tolerance in pregnancy

artículo científico publicado en 2005

HLA-G polymorphisms and soluble HLA-G protein levels in women with recurrent pregnancy loss from Basrah province in Iraq

artículo científico publicado en 2012

HLA-G: an asthma gene on chromosome 6p

artículo científico publicado en 2005

Heritability estimation and differential analysis of count data with generalized linear mixed models in genomic sequencing studies

scientific article published on 01 February 2019

Heritability estimation of sex-specific effects on human quantitative traits

artículo científico publicado en 2007

High-resolution mapping of crossovers reveals extensive variation in fine-scale recombination patterns among humans.

artículo científico publicado en 2008

High-resolution two-dimensional electrophoretic survey of serum protein genetic types in Schmiedeleut Hutterites

artículo científico publicado en 1991

Homozygous founder mutation in desmocollin-2 (DSC2) causes arrhythmogenic cardiomyopathy in the Hutterite population

artículo científico publicado en 2013

Host genetic variation in mucosal immunity pathways influences the upper airway microbiome

Host genetic variation in mucosal immunity pathways influences the upper airway microbiome.

artículo científico publicado en 2017

Host genetic variation influences gene expression response to rhinovirus infection

artículo científico publicado en 2015

Human body scents: conscious perceptions and biological effects

artículo científico publicado en 2005

Human spermatogenic failure purges deleterious mutation load from the autosomes and both sex chromosomes, including the gene DMRT1.

artículo científico publicado en 2013

IFNG genotype and sex interact to influence the risk of childhood asthma

artículo científico publicado en 2011

ITGB3 shows genetic and expression interaction with SLC6A4.

artículo científico publicado en 2006

Immune development and environment: lessons from Amish and Hutterite children

artículo científico publicado en 2017

Increased protein-coding mutations in the mitochondrial genome of African American women with preeclampsia

artículo científico publicado en 2012

Inheritance of most X-linked traits is not dominant or recessive, just X-linked

artículo científico publicado en 2004

Innate Immunity and Asthma Risk

artículo científico publicado en 2016

Innate Immunity and Asthma Risk in Amish and Hutterite Farm Children

artículo científico publicado en 2016

Integrated analyses of gene expression and genetic association studies in a founder population

artículo científico publicado en 2016

Integrated genome-wide association, coexpression network, and expression single nucleotide polymorphism analysis identifies novel pathway in allergic rhinitis

artículo científico publicado en 2014

Integration of mouse and human genome-wide association data identifies KCNIP4 as an asthma gene

artículo científico publicado en 2013

Integrin β3 genotype influences asthma and allergy phenotypes in the first 6 years of life

article

Intellectual disability associated with a homozygous missense mutation in THOC6

artículo científico publicado en 2013

Inverted duplications on acentric markers: mechanism of formation

artículo científico publicado en 2009

Lessons Learned From GWAS of Asthma.

artículo científico publicado en 2019

Leveraging gene-environment interactions and endotypes for asthma gene discovery

scientific article published on March 2016

Linkage analysis with dense SNP maps in isolated populations

artículo científico publicado en 2009

Linkage disequilibrium and age estimates of a deletion polymorphism (1597DeltaC) in HLA-G suggest non-neutral evolution.

artículo científico publicado en 2002

Loneliness is associated with sleep fragmentation in a communal society

artículo científico publicado en 2011

Longitudinal data reveal strong genetic and weak non-genetic components of ethnicity-dependent blood DNA methylation levels

scientific article published on 30 September 2020

Major loci influencing serum triglyceride levels on 2q14 and 9p21 localized by homozygosity-by-descent mapping in a large Hutterite pedigree

artículo científico publicado en 2003

Matching two independent cohorts validates DPH1 as a gene responsible for autosomal recessive intellectual disability with short stature, craniofacial, and ectodermal anomalies

artículo científico publicado en 2015

Maternal asthma and microRNA regulation of soluble HLA-G in the airway

artículo científico publicado en 2013

Maternal microchimerism protects against the development of asthma

artículo científico publicado en 2013

Meta-analysis of genome-wide association studies of asthma in ethnically diverse North American populations

artículo científico publicado en 2011

Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

artículo científico publicado en 2015

Multiancestry association study identifies new asthma risk loci that colocalize with immune-cell enhancer marks.

artículo científico publicado en 2017

Multilocus linkage disequilibrium mapping by the decay of haplotype sharing with samples of related individuals

artículo científico publicado en 2005

Mutation for nonsyndromic mental retardation in the trans-2-enoyl-CoA reductase TER gene involved in fatty acid elongation impairs the enzyme activity and stability, leading to change in sphingolipid profile

artículo científico publicado en 2013

Nasal Microbiome Composition Is Associated with Chitotriosidase (Chit1) Activity in Adult Hutterites

artículo científico publicado en 2016

Noninvasive Analysis of the Sputum Transcriptome Discriminates Clinical Phenotypes of Asthma

artículo científico publicado en 2016

Noninvasive analysis of the sputum transcriptome discriminates clinical phenotypes of asthma

artículo científico publicado en 2015

Novel case-control test in a founder population identifies P-selectin as an atopy-susceptibility locus

artículo científico publicado en 2003

PRIMAL: Fast and accurate pedigree-based imputation from sequence data in a founder population

artículo científico publicado en 2015

Parent of origin gene expression in a founder population identifies two new candidate imprinted genes at known imprinted regions

scientific article published in PLoS ONE

Parent-of-origin effects on quantitative phenotypes in a large Hutterite pedigree

Paternally inherited HLA alleles are associated with women's choice of male odor

artículo científico publicado en 2002

Pathogenic Variant in ACTB, p.Arg183Trp, Causes Juvenile-Onset Dystonia, Hearing Loss, and Developmental Delay without Midline Malformation

artículo científico publicado en 2017

Perspectives on the past decade of asthma genetics

scientific article published on 01 August 2005

Positive selection on human gamete-recognition genes

artículo científico publicado en 2018

Pregnancy outcome in recurrent miscarriage patients with skewed X chromosome inactivation

Prenatal tobacco smoke exposure is associated with childhood DNA CpG methylation

artículo científico publicado en 2014

Present status on the genetic studies of asthma

artículo científico publicado en 2002

Quantitative-trait homozygosity and association mapping and empirical genomewide significance in large, complex pedigrees: fasting serum-insulin level in the Hutterites

artículo científico publicado en 2002

Rare non-coding variants are associated with plasma lipid traits in a founder population

artículo científico publicado en 2017

Recessive TRAPPC11 mutations cause a disease spectrum of limb girdle muscular dystrophy and myopathy with movement disorder and intellectual disability

artículo científico publicado en 2013

Reducing mitochondrial reads in ATAC-seq using CRISPR/Cas9.

artículo científico publicado en 2017

Resequencing candidate genes implicates rare variants in asthma susceptibility

artículo científico publicado en 2012

Response to correspondence of NDUFS4-related Leigh syndrome in Hutterites.

artículo científico publicado en 2017

Rethinking genetic models of asthma: the role of environmental modifiers

artículo científico publicado en 2005

Rhinovirus wheezing illness and genetic risk of childhood-onset asthma

artículo científico publicado en 2013

Rising prevalence of asthma is sex-specific in a US farming population

artículo científico publicado en 2011

Risky Business: Meeting the Structural Needs of Transdisciplinary Science

artículo científico publicado en 2017

Seasonal variation in human gut microbiome composition

artículo científico publicado en 2014

Sequence variation in the IL4 gene and resistance to Trypanosoma cruzi infection in Bolivians.

artículo científico publicado en 2011

Sequence variation in the promoter region of the cholinergic receptor muscarinic 3 gene and asthma and atopy

artículo científico publicado en 2003

Sequence variations at the human leukocyte antigen-linked olfactory receptor cluster do not influence female preferences for male odors

artículo científico publicado en 2010

Sequencing the IL4 locus in African Americans implicates rare noncoding variants in asthma susceptibility

artículo científico publicado en 2009

Sex differences in the genetic basis of morning serum cortisol levels: genome-wide screen identifies two novel loci specific to women

artículo científico publicado en 2005

Sex-specific genetic architecture of asthma-associated quantitative trait loci in a founder population

scientific article published on 01 May 2006

Sex-specific genetic architecture of human disease

artículo científico publicado en 2008

Sex-specific genetic architecture of whole blood serotonin levels

artículo científico publicado en 2004

Shades of gray: a comparison of linkage disequilibrium between Hutterites and Europeans

artículo científico publicado en 2010

Shared and distinct genetic risk factors for childhood onset and adult onset asthma

Shared and distinct genetic risk factors for childhood-onset and adult-onset asthma: genome-wide and transcriptome-wide studies

scientific article published on 27 April 2019

Stress and Bronchodilator Response in Children with Asthma

artículo científico publicado en 2015

TMEM237 is mutated in individuals with a Joubert syndrome related disorder and expands the role of the TMEM family at the ciliary transition zone

artículo científico publicado en 2011

Targeted Germline Modifications in Rats Using CRISPR/Cas9 and Spermatogonial Stem Cells

artículo científico publicado en 2015

Testing for Hardy-Weinberg equilibrium in samples with related individuals

artículo científico publicado en 2004

The ABO blood group is a trans-species polymorphism in primates

artículo científico publicado en 2012

The CFTR Met 470 allele is associated with lower birth rates in fertile men from a population isolate

artículo científico publicado en 2010

The Children's Respiratory and Environmental Workgroup (CREW) birth cohort consortium: design, methods, and study population

scientific article published on 10 June 2019

The chitinase and chitinase-like proteins: a review of genetic and functional studies in asthma and immune-mediated diseases

artículo científico publicado en 2009

The combination of a genome-wide association study of lymphocyte count and analysis of gene expression data reveals novel asthma candidate genes

artículo científico publicado en 2012

The effect of freeze-thaw cycles on gene expression levels in lymphoblastoid cell lines

artículo científico publicado en 2014

The effects of EBV transformation on gene expression levels and methylation profiles ⬇️

artículo científico publicado el 2 de febrero de 2011

The effects of EBV transformation on gene expression levels and methylation profiles.

artículo científico publicado en 2012

The genetics of asthma and allergic disease: a 21st century perspective

artículo científico publicado en 2011

The maternal HLA-G 1597ΔC null mutation is associated with increased risk of pre-eclampsia and reduced HLA-G expression during pregnancy in African-American women

artículo científico publicado en 2012

The role of environmental tobacco smoke in genetic susceptibility to asthma

artículo científico publicado en 2004

The role of local CpG DNA methylation in mediating the 17q21 asthma-susceptibility GSDMB/ORMDL3 expression quantitative trait locus

artículo científico publicado en 2018

The sex-specific genetic architecture of quantitative traits in humans

artículo científico publicado en 2006

Two variants on chromosome 17 confer prostate cancer risk and the one in TCF2 protects against type 2 diabetes

article

Two-stage genome-wide association study of chronic rhinosinusitis and disease subphenotypes highlights mucosal immunity contributing to risk

artículo científico publicado en 2021

Ultra-fast local-haplotype variant calling using paired-end DNA-sequencing data reveals somatic mosaicism in tumor and normal blood samples

artículo científico publicado en 2016

Variants in DENND1A are associated with polycystic ovary syndrome in women of European ancestry

artículo científico publicado en 2012

Variants in DPF3 and DSCAML1 are associated with sperm morphology

artículo científico publicado en 2013

Variation in ITGB3 has sex-specific associations with plasma lipoprotein(a) and whole blood serotonin levels in a population-based sample

artículo científico publicado en 2005

Variation in ITGB3 is associated with asthma and sensitization to mold allergen in four populations

artículo científico publicado en 2005

Variation in ITGB3 is associated with whole-blood serotonin level and autism susceptibility

artículo científico publicado en 2006

Variation in conserved non-coding sequences on chromosome 5q and susceptibility to asthma and atopy.

artículo científico publicado en 2005

Variation in the HLA-G Promoter Region Influences Miscarriage Rates ⬇️

artículo científico publicado el 29 de abril de 2003

Variation in the type I interferon gene cluster on 9p21 influences susceptibility to asthma and atopy

scientific article published on 01 March 2006

Whole-genome sequencing of individuals from a founder population identifies candidate genes for asthma

artículo científico publicado en 2014

XM: association testing on the X-chromosome in case-control samples with related individuals

artículo científico publicado en 2012

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